Author:
dos Santos Wayler S.,Carmo Éder J.,Mendez-González Yanela,Nascimento Lucas L.,Patrocínio Antônio O. T.,Guo Ruyan,Bhalla Amar S.,M’Peko Jean-Claude,Guerra José D. S.
Abstract
AbstractElectrochemical cells for direct conversion of solar energy to electricity (or hydrogen) are one of the most sustainable solutions to meet the increasing worldwide energy demands. In this report, a novel and highly-efficient ternary heterojunction-structured Bi4O7/Bi3.33(VO4)2O2/Bi46V8O89 photoelectrode is presented. It is demonstrated that the combination of an inversion layer, induced by holes (or electrons) at the interface of the semiconducting Bi3.33(VO4)2O2 and Bi46V8O89 components, and the rectifying contact between the Bi4O7 and Bi3.33(VO4)2O2 phases acting afterward as a conventional p–n junction, creates an adjustable virtual p–n–p or n–p–n junction due to self-polarization in the ion-conducting Bi46V8O89 constituent. This design approach led to anodic and cathodic photocurrent densities of + 38.41 mA cm–2 (+ 0.76 VRHE) and– 2.48 mA cm–2 (0 VRHE), respectively. Accordingly, first, this heterojunction can be used either as photoanode or as photocathode with great performance for artificial photosynthesis, noting, second, that the anodic response reveals exceptionally high: more than 300% superior to excellent values previously reported in the literature.
Publisher
Springer Science and Business Media LLC
Cited by
5 articles.
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